Predictive value of food sensitization and filaggrin mutations in children with eczema

J Allergy Clin Immunol. 2011 Dec;128(6):1235-1241.e5. doi: 10.1016/j.jaci.2011.09.014. Epub 2011 Oct 26.

Abstract

Background: It was reported that in infants with eczema and food sensitization, the presence of a filaggrin (FLG) null mutation predicts future asthma with a specificity and positive predictive value of 100%.

Objectives: We sought to evaluate the predictive value of food sensitization and food allergy, FLG haploinsufficiency, and their combination in infants with early-onset eczema for persistent eczema and childhood asthma.

Methods: The German Infant Nutritional Intervention (GINI) and Influence of Lifestyle-related Factors on the Immune System and the Development of Allergies in Childhood (LISA) birth cohorts, as well as a collection of 65 cases of early-onset eczema with and without food allergy were investigated.

Results: The risk for asthma was significantly increased by food sensitization (positive diagnostic likelihood ratios [PLRs] of 1.9 [95% CI, 1.1-3.4] in the GINI cohort and 5.5 [95% CI, 2.8-10.8] in the LISA cohort) and the presence of an FLG mutation (PLRs of 2.9 [95% CI, 1.2-6.6] in the GINI cohort and 2.8 [95% CI, 1.0-7.9] in the LISA cohort) with a rather high specificity (79.1% and 92.9% in the GINI cohort and 89.0% and 91.7% in the LISA cohort, respectively) but low sensitivity (40.0% and 39.3% in the GINI cohort and 31.6% and 23.5% in the LISA cohort, respectively). Likewise, the risk for persistent eczema was increased. In the clinical cases neither food allergy nor FLG mutations had a significant effect. The combination of both parameters did not improve prediction and reached positive predictive values of 52.3% (GINI cohort), 66.9% (LISA cohort), and 30.6% (clinical cases), assuming an asthma prevalence in children with early eczema of 30%.

Conclusion: Early food sensitization and the presence of an FLG mutation in infants with early eczema increase the risk for later asthma, but the combination of the 2 factors does not represent a clinically useful approach to reliably identify children at risk.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asthma / complications
  • Asthma / genetics*
  • Asthma / immunology
  • Child, Preschool
  • Cohort Studies
  • Eczema / complications
  • Eczema / genetics*
  • Eczema / immunology
  • Female
  • Filaggrin Proteins
  • Food Hypersensitivity / complications
  • Food Hypersensitivity / genetics*
  • Food Hypersensitivity / immunology
  • Genetic Predisposition to Disease*
  • Humans
  • Infant
  • Infant, Newborn
  • Intermediate Filament Proteins / genetics*
  • Male
  • Mutation
  • Predictive Value of Tests
  • Randomized Controlled Trials as Topic
  • Risk Factors

Substances

  • FLG protein, human
  • Filaggrin Proteins
  • Intermediate Filament Proteins